Следене
Charles Schwartz
Charles Schwartz
Director of Research, Greenwood Genetic Center
Потвърден имейл адрес: ggc.org
Заглавие
Позовавания
Позовавания
Година
Recurrent rearrangements of chromosome 1q21. 1 and variable pediatric phenotypes
HC Mefford, AJ Sharp, C Baker, A Itsara, Z Jiang, K Buysse, S Huang, ...
New England Journal of Medicine 359 (16), 1685-1699, 2008
8352008
Singular-value decomposition and the Grassberger-Procaccia algorithm
AM Albano, J Muench, C Schwartz, AI Mees, PE Rapp
Physical review A 38 (6), 3017, 1988
7151988
A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation
PS Tarpey, R Smith, E Pleasance, A Whibley, S Edkins, C Hardy, ...
Nature genetics 41 (5), 535-543, 2009
6812009
Electron scattering from hydrogen
C Schwartz
Physical Review 124 (5), 1468, 1961
6481961
A recurrent 15q13. 3 microdeletion syndrome associated with mental retardation and seizures
AJ Sharp, HC Mefford, K Li, C Baker, C Skinner, RE Stevenson, ...
Nature genetics 40 (3), 322-328, 2008
6452008
Importance of angular correlations between atomic electrons
C Schwartz
Physical Review 126 (3), 1015, 1962
5921962
Theory of hyperfine structure
C Schwartz
Physical Review 97 (2), 380, 1955
5291955
Uniparental paternal disomy in a genetic cancer-predisposing syndrome
I Henry, C Bonaiti-Pellie, V Chehensse, C Beldjord, C Schwartz, ...
Nature 351 (6328), 665-667, 1991
5241991
Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases
HAF Stessman, BO Xiong, BP Coe, T Wang, K Hoekzema, M Fenckova, ...
Nature genetics 49 (4), 515-526, 2017
5102017
SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1–SIX1–DNA complexes
RG Ruf, PX Xu, D Silvius, EA Otto, F Beekmann, UT Muerb, S Kumar, ...
Proceedings of the National Academy of Sciences 101 (21), 8090-8095, 2004
4952004
Localized mutations in the gene encoding the cytoskeletal protein filamin A cause diverse malformations in humans
SP Robertson, SRF Twigg, AJ Sutherland-Smith, V Biancalana, RJ Gorlin, ...
Nature genetics 33 (4), 487-491, 2003
4662003
High frequency of neurexin 1β signal peptide structural variants in patients with autism
J Feng, R Schroer, J Yan, W Song, C Yang, A Bockholt, EH Cook Jr, ...
Neuroscience letters 409 (1), 10-13, 2006
4012006
Allan-Herndon-Dudley syndrome and the monocarboxylate transporter 8 (MCT8) gene
CE Schwartz, MM May, NJ Carpenter, RC Rogers, J Martin, MG Bialer, ...
The American Journal of Human Genetics 77 (1), 41-53, 2005
3832005
Isolation and characterization of the faciogenital dysplasia (Aarskog-Scott syndrome) gene: a putative RhoRac guanine nucleotide exchange factor
NG Pasteris, A Cadle, LJ Logie, MEM Porteous, CE Schwartz, ...
Cell 79 (4), 669-678, 1994
3791994
A multicenter study on genotype-phenotype correlations in the fragile X syndrome, using direct diagnosis with probe StB12. 3: the first 2,253 cases
F Rousseau, D Heitz, J Tarleton, J MacPherson, H Malmgren, N Dahl, ...
American journal of human genetics 55 (2), 225, 1994
3691994
X Chromosome–inactivation patterns of 1,005 phenotypically unaffected females
JM Amos-Landgraf, A Cottle, RM Plenge, M Friez, CE Schwartz, ...
The American Journal of Human Genetics 79 (3), 493-499, 2006
3642006
A promoter mutation in the XIST gene in two unrelated families with skewed X-chromosome inactivation
RM Plenge, BD Hendrich, C Schwartz, JF Arena, A Naumova, C Sapienza, ...
Nature genetics 17 (3), 353-356, 1997
3451997
Center-of-mass motion in many-particle systems
S Gartenhaus, C Schwartz
Physical Review 108 (2), 482, 1957
3401957
5, 10 Methylenetetrahydrofolate reductase genetic polymorphism as a risk factor for neural tube defects
CY Ou, RE Stevenson, VK Brown, CE Schwartz, WP Allen, MJ Khoury, ...
American journal of medical genetics 63 (4), 610-614, 1996
3221996
Lamb shift in the helium atom
C Schwartz
Physical Review 123 (5), 1700, 1961
3121961
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Статии 1–20